Clinical trial

Immunogenicity and Safety Study of a Third Vaccination With FSME-IMMUN 0.5 mL in…

NCT00163540 · Pfizer, Industry · Completed

Key facts

NCT number NCT00163540
Title Immunogenicity and Safety Study of a Third Vaccination With FSME-IMMUN 0.5 mL in Subjects Previously Vaccinated According to a Rapid Immunization Schedule (Follow-up to Study 225)
Official title Open-Label, Follow-up, Phase IV Clinical Study to Evaluate the Immunogenicity and Safety of a Third Vaccination With FSME-IMMUN 0.5 mL in Subjects Previously Vaccinated Using a Rapid Immunization Schedule (Follow-up to Study 225)
Lead sponsor Pfizer, Industry
Status Completed
Phase Phase 4
Study type Interventional
Conditions Encephalitis, Tick-borne
Intervention type Biological
Interventions Formaldehyde inactivated, sucrose gradient purified TBE virus antigen, strain Neudörfl
Start date May 1, 2005
Completion Jun 1, 2005
First posted Sep 14, 2005
Last update posted May 21, 2015
Countries Belgium

At a glance

  • 1–9 Study sites
  • No Results posted
  • None Linked FDA submissions

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

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Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date:

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